|
|
||||||||
From the University Eye Clinic, Basel, Switzerland.
| Abstract |
|---|
|
|
|---|
METHODS. Five measurements of choroidal blood flow were obtained on 5 days in both eyes of 10 subjects. Reliability, sensitivity, and sample size calculations were performed. Yield, the intensity of the returning light (direct current [DC]) divided by the signal amplification (gain) used during recording, was calculated (yield = DC/gain). The correlation between yield and the LDF parameters velocity, volume, and flux was analyzed. Reliability, sensitivity, and sample size calculations were repeated after correcting for this relationship. The influence of different light-scattering properties on the returning signal was assessed in a model eye.
RESULTS. Yield and the LDF parameters, velocity, volume, and flux, correlated significantly in a regression model. After the influence of yield was partialized out, reliability, reproducibility, sensitivity, and statistical power improved markedly. The high reliability of yield in a given eye (87%) suggests, that, besides varying recording settings on different days, individual specific scattering properties within the eye influence LDF measurements. Comparison of model eye data with human data disclosed a low signal-to-noise ratio with decreasing yield. Correcting for yield did not affect the sensitivity to blood flow changes induced by hypercapnia or a suction cup.
CONCLUSIONS. Tissue-scattering properties alter the characteristics of the returning light, and recording settings affect the outcome of the analysis of the returning light during LDF measurements. Partializing out the influence of yield markedly improves the reproducibility of choroidal LDF.
| Introduction |
|---|
|
|
|---|
Laser Doppler flowmetry (LDF) has repeatedly been applied for the assessment of choroidal blood flow in humans.14 15 16 17 18 19 The marked variability of measurements obtained with this technology precludes a wide application of this methodology. In a preparation devoid of nonblood-flowrelated movement, this variation is thought to be due to variation in vascular density and vessel orientation within the relatively small volume of tissue sampled by LDF. In the present study, we investigated the sources of the variation during choroidal LDF, using a new compact, confocal choroidal laser Doppler flowmeter (Institut de Recherche en Ophtalmologie, Sion, Switzerland).15 This instrument was used in the present study, because, theoretically, it comes close to the assumption that the site of LDF measurement does not change between measurements.
| Subjects and Methods |
|---|
|
|
|---|
The optical system for the delivery of the laser beam and the detection
of the scattered light of the new compact, confocal choroidal laser
Doppler flowmeter (Institut de Recherche en Ophtalmologie) is based on
a confocal arrangement and has been described in detail
elsewhere.15
Briefly, a polarized laser source (
=
785 nm, 100 µm) is relayed with a 1:1 optical system (laser beam at
the cornea: width, 1.3 mm; power, 90 µW) and focused at the
subjects retina (spot in the retinal image plane, 1020 µm in
diameter; optical thickness of confocal layer, 300 µm). The point
laser source, the point of illumination of the fovea, and the detecting
optical fiber are located in conjugated planes. The scattered light is
collected by an optical system organized with six fibers arranged
circularly around the central fixation point along a circle of diameter
of 180 µm (within the avascular zone of the fovea).
Subjects
Ten healthy nonsmoking volunteers (seven women, three men; age,
2438 years; mean ± SD, 33.17 ± 3.9) were recruited. The
procedures were approved by the local ethics committee, the tenets of
Declaration of Helsinki were observed, and each subject signed an
informed consent form before undergoing examination. Included were
individuals with no history of ocular or systemic disease, no history
of long-term or current use of systemically active or topical
medication, and no history of drug or alcohol abuse. Further inclusion
criteria were normal systolic (100140 mm Hg) and diastolic (6090 mm
Hg) blood pressure, best corrected visual acuity of more than 20/25 in
both eyes, ametropia within -3 to + 3 D of spherical equivalent and
less than 1 D astigmatism in both eyes, pupil diameter of at least 4
mm, applanatory intraocular pressure (IOP) below 20 mm Hg in both eyes,
and no pathologic findings in slit lamp examination and indirect
fundoscopy.
Measurement of the Blood Flow Parameters
Subjects were examined after an overnight fast and were asked to
refrain from alcohol and caffeine for 12 hours before the trial days. A
resting period of at least 30 minutes was scheduled for each subject.
Stable baseline conditions were established and were ensured by
repeated measurements of blood pressure. The subjects were seated with
the head stabilized in a slit lamp headrest. Care was taken to
standardize the subjects head position by aligning marks on the
headrest with anatomic landmarks on the forehead, chin, and temporal
orbital rim. The subjects were asked to fixate the red-light spot
within the ocular and to adjust the focus by turning the ocular until
the smallest possible size of the red light spot was obtained. The
ocular-to-cornea distance was set between 1.5 and 2 cm and held
constant in all the subsequent recordings. In addition, constant, very
low-level artificial room illumination was used throughout all the
experiments. Twenty- to 25-second recordings were obtained in each eye.
A stable direct current (DC) during a recording was used as a criterion
for proper fixation. All subjects were perfectly familiar with the
measurement technique.
Reproducibility of the Measurements
Five measurements of choroidal blood flow were obtained in both
eyes of 10 subjects on five consecutive days. All the measurements were
performed at the same time of day in each subject (±15 minutes). Right
and left eyes were measured in random order. Once a recording was
obtained and saved, no further analysis was attempted until the end of
data collection in all the scheduled examinations. Consequently, the
examiner (KG) was masked to the previous measurement results of a given
subject. The intraindividual (repeated measurements in the same eye)
coefficients of variation (CV = 100 x SD/mean) were
assessed. The reliability (R, intraclass correlation
coefficient) was assessed according to the formula21
![]() |
Detection Sensitivity of the Blood Flow Parameters
The minimum statistically significant change (S) that
can be detected in a group of 10 subjects was calculated according to
the formula21
![]() |
Sample Size Calculations
Sample size calculations for a change of 5%, 10%, 15%, and
25% from baseline were performed for the parameter flux, with the
error set to 0.05 and the power (1-ß) set to 0.8. A range of sample
size calculations was calculated by comparing the first recordings to
the series that followed.
Correlation between Right and Left Eyes
The correlation between the measurements in the right and the
left eyes was assessed for all the parameters by means of Pearsons
correlation factor (50 pairs of measurements).
Influence of the Return Light Intensity
In LDF, the main expression of the intensity of the returning
light is the mean DC level. The main expression of the part of the
signal containing both the information pertaining to blood flow and
noise is the root mean square (RMS) of the voltages, or the alternating
current (AC) component. Blood flow parameters are calculated after
computing a Doppler-shift power spectrum of the returning signal. The
LDF parameters volume and flux, which are derived from the area under
the curve of the Doppler-shift power spectrum, are standardized with
DC2
(DC squared). Velocity is a ratio of flux and volume.
The algorithm of the instrument requires DC levels to range between 0.5
and 5 V, which is achieved through amplification of the photocurrent.
This amplification can take the following discrete values (gain): 1, 2,
5, 10, 20, and 50. Because the necessity for amplification may be
related to scattering properties of the sampled tissue, and because the
same tissue properties may also alter the computed LDF parameters, a
new parameter, yield = DC/gain, was defined, and the relationship
between yield and the LDF parameters velocity, volume, and flux were
analyzed. The influence of yield on the recorded LDF parameters was
partialized out in a regression model (third-order polynomial equation)
applied on the logarithmic values of yield and LDF parameters.
Reliability, sensitivity, and sample size calculations were repeated
after partializing out the influence of yield.
The correlation between yield in the right and the left eyes was assessed by means of Pearsons correlation factor between all measurements in the right and left eyes (50 pairs of measurements). The reliability (R, intraclass correlation coefficient) for yield in a given eye as well as in an individual (average yield for both eyes) was calculated.
Influence of Different Light-Scattering Properties
The influence of different light-scattering properties on the
returning signal was assessed in an emmetropic model eye. Although LDF
recordings in such a model eye give rise to a Doppler-shift power
spectrum similar to those obtained from the choroid, the AC component
of the signal consists only of noise, because there is no flow or
motion. In this model eye, materials with various light-scattering
properties (mono- and multilayers of semitransparent plastic folio and
dyed cloths) were placed at the fundus level, and recordings were
obtained without any movement and without any change in the recording
settings. A range of return light intensities comparable to those
observed in humans was produced by merely changing the scattering
material at the fundus level. After dividing recorded RMS with gain,
the obtained variable was plotted against yield, providing a graphical
representation of the noise level at various yield levels. A similar
plot (RMS/gain versus yield) was obtained for human data and the two
plots were fitted by a least-squares regression line, depicting
graphically the relative contribution of noise in the measurements
obtained in human eyes.
Influence of Correction on Blood Flow Measurement
To test the influence of the correction on the results obtained
during blood flow perturbation, the choroidal LDF parameter flux was
recorded under the following conditions: in two subjects, at baseline,
and after various steps of increased IOP induced by means of a Langham
suction cup (10 mm in diameter and a volume of 0.3 mL), and in two
subjects, while they breathed a mixture of room air and 5%
CO2 through a partly closed mask system covering
both mouth and nose connected to a CO2 monitor
(Capnomac Ultima; AVL Medical Systems AG, Schaffhausen, Switzerland)
for approximately 15 minutes. In the latter situation, end-tidal
CO2 concentrations were monitored continuously
during room air breathing and during exposure to increased inspiratory
CO2 concentrations. The relative change in blood
flow was calculated with the unaltered and the corrected values
obtained after applying the procedure just described.
| Results |
|---|
|
|
|---|
Although choroidal LDF measurements were always performed on the same spot (foveola), the comparison of returning lights intensity and LDF flux values disclosed a marked variability in DC and flux values, as well as an inverse relationship between these two parameters (Fig. 1) .
|
|
|
|
error
0.05) improved significantly (area under the curve:
P < 0.0001) after correcting for the influence of
yield (Fig. 5)
.
|
|
|
|
| Discussion |
|---|
|
|
|---|
The indirect mode of measurement used in the present study as well as the confocal optical arrangement in the present device favor choroidal blood flow measurements.15 According to Riva et al.,14 even in the direct mode of measurement, the contribution of the retinal capillaries during measurements within the foveola is approximately one eighth of the signal. With the indirect mode, the Doppler-shift power spectra have an exponential shape and a relatively low mean pulsatility, corresponding to a capillary vascular bed, and, thus, lending support to the assumption that the signal obtained with this method originates mostly from the choriocapillaris with little, if any, contribution form the deep feeder vessels of the choroid.14
The two main sources of variability of returning light intensity seem to be light-scattering properties of the sampled tissue volume and the alignment between the instrument and the eye. In the present study, each eye had systematically a different yield range compared with other eyes, reliability coefficient for yield for eyes was 87%, but this was also the case in subjects, indicated by a reliability coefficient of 78% and interocular yield correlation. These findings suggest that yield is in part defined by tissue optical properties, expectedly similar in eyes of the same person. Such an interpretation is also strengthened by the fact that the instrument used in the present study comes close to the assumption that the site of LDF measurement (foveola) does not change between recordings.
The exact mechanism of the observed systematic dependence of LDF parameters on the returning light intensity is not clear. The major issues demonstrated in the present experiments were the alteration of the signal within eyes in the low-yield range and the dramatic increase of the relative noise contribution in the low-signal range. A possible explanation of how parameters normalized with DC (volume and flux) might be affected could be the presence of specular reflection, as observed in some other LDF applications.24 Because specular light is not shifted in frequency, it will contribute only to the DC component. However, an optical confocal arrangement, an indirect mode of measurement, and the use of polarizing filters make specular light as the major source of the observed phenomenon a remote possibility. Another speculation may be an inadequate existing DC2 -normalization algorithm for volume and flux, and some exponential factor other than 2 might be more appropriate. Explanation of the underlying physical phenomena necessitates further investigations. Empiric correction removed a large part of LDF parameter variability not directly related to blood flow, and such a correction did not partialize the information pertaining to changes in blood flow, as demonstrated in measurements during hypercapnia after increasing IOP by means of a suction cup.
The experiments with blood flow challenge warrant some additional explanation. An increase in IOP of 12 mm Hg reduced choroidal blood flow by 30% to 40% in one of the subjects, which compares well with the range of choroidal blood flow responses found in a study demonstrating blood flow autoregulation in the human choroid.25 However, the even larger decrease in choroidal blood flow with higher IOP suggests that this subject may have an altered choroidal blood flow autoregulation. A detailed discussion of this issue would be beyond the scope of the present study. It should, nevertheless, be noted that all subjects whose choroidal blood flow was challenged in this study were completely healthy; but, obviously, autoregulatory capacity for choroidal blood flow was not comparable among them. To the best of our knowledge, altered autoregulation alone does not necessarily represent a noxious state. Many young subjects have altered autoregulation in the cerebral,26 the retinal,27 or the choroidal (Hasler et al., manuscript submitted) circulation without being in poor health. Prospective studies should evaluate the impact of altered autoregulation on long-term health. When the data obtained during hypercapnia are compared with baseline measurements, the results after correcting for yield show a difference of 8% to 9% compared with the result before correction. During continuous measurements, a change of less than 8% from baseline should not be considered relevant.14 This limit should certainly be even higher for repeated measurements. Consequently, the choroidal blood flow change estimates before and after correcting for yield can be considered comparable. Furthermore, an average increase of 1.5% in choroidal LDF flux per 1 mm Hg increase in partial pressure of CO2 has been described in healthy subjects.19 The expected increase in LDF parameter flux in our two subjects amounted to 23.6% and 15.8%. Because of the large confidence interval suggested by the figures provided in the latter study (approximately ±15%), the responses found in our two subjects, especially after correcting for yield, match well the expected change during hypercapnia.
Interindividual comparisons of baseline values are generally not recommended in LDF techniques, primarily because of varying tissue-scattering properties. If, however, these properties could find their quantitative expression in the returning light intensity, as suggested by the present data, perhaps it would be feasible to universally correct for their influence based on a sufficiently large choroidal blood flow LDF recording database and thus to enable and enhance interindividual comparisons. However, even the results of a conservative study design, which would include comparisons of baseline and follow-up measurements in the same eye, may be jeopardized by the influence of instrument alignment, particularly if baseline and follow-up measurements are performed in separate sessions. In the present study, although care was taken to reproduce accurately the recording conditions in each session, empiric correction was still warranted, suggesting that similar corrections should be run regularly. Finally, although the instrument used in this study has some special characteristics different from other continuous LDF instrumentsconfocal arrangement, indirect mode of measurementit seems plausible to admit that the issues raised here may be at least partly valid for other widely used continuous LDF instrument applications and possible also scanning LDF instruments, such as the Heidelberg Retina Flowmeter (Heidelberg Engineering, Heidelberg, Germany)28 a conjecture that should, however, be verified.
| Footnotes |
|---|
Submitted for publication March 21, 2001; revised September 4, 2001; accepted November 1, 2001.
Commercial relationships policy: N.
The publication costs of this article were defrayed in part by page
charge payment. This article must therefore be marked
"advertisement" in accordance with 18 U.S.C.
1734
solely to indicate this fact.
Corresponding author: Selim Orgül, University Eye Clinic Basel, Mittlere Strasse 91, PO Box CH-4012, Basel, Switzerland; sorgul{at}magnet.ch
| References |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
K. Polak, A. Luksch, F. Berisha, G. Fuchsjaeger-Mayrl, S. Dallinger, and L. Schmetterer Altered Nitric Oxide System in Patients With Open-Angle Glaucoma Arch Ophthalmol, April 1, 2007; 125(4): 494 - 498. [Abstract] [Full Text] [PDF] |
||||
![]() |
P Kaeser, S Orgul, C Zawinka, G Reinhard, and J Flammer Influence of change in body position on choroidal blood flow in normal subjects Br. J. Ophthalmol., October 1, 2005; 89(10): 1302 - 1305. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Gugleta, S. Orgul, P. Hasler, and J. Flammer Circulatory Response to Blood Gas Perturbations in Vasospasm Invest. Ophthalmol. Vis. Sci., September 1, 2005; 46(9): 3288 - 3294. [Abstract] [Full Text] [PDF] |
||||
![]() |
E Polska, K Polak, A Luksch, G Fuchsjager-Mayrl, V Petternel, O Findl, and L Schmetterer Twelve hour reproducibility of choroidal blood flow parameters in healthy subjects Br. J. Ophthalmol., April 1, 2004; 88(4): 533 - 537. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Polska, P. Ehrlich, A. Luksch, G. Fuchsjager-Mayrl, and L. Schmetterer Effects of Adenosine on Intraocular Pressure, Optic Nerve Head Blood Flow, and Choroidal Blood Flow in Healthy Humans Invest. Ophthalmol. Vis. Sci., July 1, 2003; 44(7): 3110 - 3114. [Abstract] [Full Text] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |